Canonical Allele Identifier: CA2815053034
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470918G>C , CM000682.2:g.2470918G>C GRCh38
NC_000020.10:g.2451564G>C , CM000682.1:g.2451564G>C GRCh37
NC_000020.9:g.2399564G>C NCBI36
NG_042057.1:g.4936C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3160C>G ENSP00000456213.1:n.305-3160C>G